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Dr.Hana's Nasopure Nasal Wash Refill Kit - 80 ct

by NeilMed Pharmaceuticals Inc.

Ref 5003FAN-NP-USModel 890668000128, 890668000067

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00890668000128 Basic UDI-DI Date31 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Trade Name
Dr.Hana's Nasopure Nasal Wash Refill Kit - 80 ct
Dr.Hana's Nasopure Nasal Wash Refill Kit - 40 ct
Device Name
Dr.Hana's Nasopure Nasal Wash Refill Kit
Model / Reference
890668000128, 5003FAN-NP-US, 890668000067
Primary DI / UDI-DI
00890668000128, 00890668000067
Basic UDI-DI
B-00890668000128, B-00890668000067
EMDN Code
Q030103 Nasal irrigation solutions
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000025412
Authorised representative
MDSS GmbH DE-AR-000005430

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Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No